• 제목/요약/키워드: cox3

검색결과 1,637건 처리시간 0.026초

Thymoquinone (TQ) regulates cyclooxygenase-2 expression and prostaglandin E2 production through PI3kinase (PI3K)/p38 kinase pathway in human breast cancer cell line, MDA-MB-231

  • Yu, Seon-Mi;Kim, Song-Ja
    • Animal cells and systems
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    • 제16권4호
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    • pp.274-279
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    • 2012
  • Thymoquinone (TQ), a drug extracted from the black seeds of Nigella sativa, has been shown to exhibit anti-inflammatory, anti-oxidant, and anti-neoplastic effects in numerous cancer cells. The effects of TQ on cyclooxygenase-2 (COX-2) expression and prostaglandin $E_2$ ($PGE_2$) production in MDA-MB-231, however, remain poorly understood. Western blot analysis and immunofluorescence staining were performed to study the expression levels of inflammation regulatory proteins in MDA-MB-231. $PGE_2$ assay was conducted to explore the TQ-induced production of $PGE_2$. In this study, we investigated the effects of TQ on COX-2 expression and $PGE_2$ production in MDA-MB-231. TQ significantly induced COX-2 expression and increased $PGE_2$ production in a dose-dependent manner, as determined by a Western blot analysis and $PGE_2$ assay. Furthermore, the activation of Akt and p38 kinase, respectively, was up-regulated in TQ treated cells. Inhibition of p38 kinase with SB203580 and PI3kinase (PI3K) with LY294002 abolished TQ-caused COX-2 expression and decreased $PGE_2$ production. These results collectively demonstrate that TQ effectively modulates COX-2 expression and $PGE_2$ production via PI3K and p38 kinase pathways in the human breast cancer cell line MDA-MB-231.

림프절 전이를 동반한 직장암 환자들에서 Cyclooxygenase-2 발현의 임상적 의미 (Clinical Implication of Cyclooxygenase-2 Expression for Rectal Cancer Patients with Lymph Node Involvement)

  • 이형식;최영민;허원주;김수진;김대철;노미숙;홍영습;박기재
    • Radiation Oncology Journal
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    • 제27권4호
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    • pp.210-217
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    • 2009
  • 목 적: 림프절 전이가 동반된 직장암 환자들에서 cyclooxygenase-2 (COX-2) 발현이 생존율에 미치는 영향을 조사 하고자 한다. 대상 및 방법: 1998년부터 2004년까지 직장암으로 동아대병원에서 근치적 수술과 수술 후 방사선치료를 받은 환자들 중에서 림프절 전이가 동반된 경우를 대상으로 후향적분석을 하였다. 86명 중에서 수술 후 조직을 찾을 수 없는 3명, 악성 흑색종 1명, 진단 전후 2년 내에 위암과 폐암이 발생한 각 1명, 진단 시에 간 전이가 있었던 1명, 720 cGy 후 방사선치료를 거부한 1명 등을 제외한 78명을 대상으로 분석하였다. COX-2에 대한 면역조직화학염색은 자동면역염색기로 하였고, 스캔한 후, 영상분석기를 이용하여 분석하였다. Kaplan-Meier 생존율 분석을 하였고, Log rank 검사로 유의성을 조사하였다. 결 과: 면역조직화학염색에서 COX-2 양성이 62명(79.5%), 음성이 16명(20.5%)이었고, 양성도가 1, 2, 3인 환자들이 각각 6명(7.7%), 15명(19.2%), 41명(52.6%)이었다. 환자의 나이(60세 미만, 이상), 성별, 수술 방법(복회음절제술, 하위전방절제술), 세포의 분화도, 종양의 크기(5 cm 미만, 5 cm 이상), T병기, N병기, 병기(IIIa, IIIb, IIIc), 등에 따른 COX-2 발현의 차이는 없었다. 전체 환자의 5년 생존율과 무병생존율은 각각 57.0%, 51.6%였다. COX-2 음성과 양성인 환자들의 5년 생존율이 72.9%와 53.0% (p=0.146), 5년 무병생존율이 72.7%와 46.3% (p=0.118)였다. COX-2 양성도가 0, 1, 2, 3인 환자들의 5년 생존율은 각각 72.9, 50.0 51.3, 53.1%였고(p=0.495), 5년 무병생존율은 각각 72.7, 50.0, 46.7, 45.1%였다(p=0.451). 5년 생존율은 악성종양 세포의 분화도, N병기, 병기, 등에 따라서, 5년 무병생존율은 N병기, 병기, 등에 따라서 유의한 차이가 있었다(p<0.05). 결 론: 림프절 전이가 동반된 직장암 환자에서 COX-2의 발현 여부와 정도는 생존율에 유의한 영향을 주지는 않았다. 하지만 향후 보다 많은 환자군을 대상으로 연구하여, COX-2 발현이 직장암의 예후에 미치는 영향을 규명해야 할 것으로 생각된다.

감마선조사에 의한 돼지 피부장애에 cyclooxygenase-2의 발현변화 (Gamma-ray-induced skin injury in the mini-pig: Effects of irradiation exposure on cyclooxygenase-2 expression in the skin)

  • 김중선;박선후;장원석;이선주;이승숙
    • Journal of Radiation Protection and Research
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    • 제40권1호
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    • pp.65-72
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    • 2015
  • 방사선 노출에 따른 피부손상의 기본이론들은 정립되어 있지만, 정확한 기전에 관해서는 알려지지 않은 실정이다. 본 연구에서는 감마선 조사 후 용량 및 시간에 따라 돼지 피부의 장애를 육안 및 조직학적인 변화를 통해 평가하고 cyclooxygenase(COX)-2 발현 정도를 비교하고자 하였다. 미니돼지의 등 쪽 피부에 20-70 Gy 감마선을 국소조사 후 12 주 동안 육안적인 변화를 관찰하고 생검을 통해 조직학적인 변화를 관찰하였다. 방사선 조사 후 피부의 기저세포층에서의 세포자멸사와 표피층의 두께 변화를 평가하였고 COX-2 발현 정도를 면역염색을 통하여 비교하였다. 방사선 조사 후 피부 장애는 용량이 증가할수록 피부손상이 더욱 심하였으며 초기에 발적 소견을 보이다가 50 Gy 이상 조사군에서는 미란과 궤양으로 이어졌다. 조직학적인 변화는 육안적인 소견과 일치하였다. 방사선 조사 후 3일부터 기저세포에서 세포자멸사가 관찰되었으며 기저세포수의 감소가 유발되었으며 이러한 변화는 용량이 증가할수록 더욱 증가하였다. 방사선 조사 후 표피층의 두께는 3일 무렵에 일시적으로 증가하다가 점차 감소하였으며 20, 30, 40 Gy 조사 군에서는 다시 회복되는 소견이 관찰되었으나 50, 70 Gy 조사 군에서는 다시 회복되지 못하고 표피창의 두께 소실을 보였다. 방사선 조사 후 피부에서의 COX-2 발현은 피부손상정도와 일치하게 관찰되었다. 방사선 조사 후 COX-2 발현은 방사선의 용량이 증가할수록 발현이 증가하였고 시간이 증가할수록 증가하였다. 이러한 조직학적인 변화와 함께 방사선 손상을 일으키는 신호전달에 관여하는 COX-2 발현이 방사선조사 용량에 비례하여 증가하며 이러한 단백질의 발현은 피부손상과 관련성이 높은 것으로 사료된다.

Salicylate Regulates Cyclooxygenase-2 Expression through ERK and Subsequent $NF-_kB$ Activation in Osteoblasts

  • Chae, Han-Jung;Lee, Jun-Ki;Byun, Joung-Ouk;Chae, Soo-Wan;Kim, Hyung-Ryong
    • The Korean Journal of Physiology and Pharmacology
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    • 제7권4호
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    • pp.239-246
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    • 2003
  • The expression of cyclooxygenase-2 (COX-2) is a characteristic response to inflammation and can be inhibited with sodium salicylate. $TNF-{\alpha}$ plus $IFN-{\gamma}$ can induce extracellular signal-regulated kinase (ERK), IKK, $I{\kappa}B$ degradation and NF-${\kappa}B$ activation. The inhibition of the ERK pathway with selective inhibitor, PD098059, blocked cytokine-induced COX-2 expression and $PGE_2$ release. Salicylate treatment inhibited COX-2 expression induced by $TNF-{\alpha}$/$IFN-{\gamma}$ and regulated the activation of ERK, IKK and $I{\kappa}B$ degradation and subsequent NF-${\kappa}B$ activation in MC3T3E1 osteoblasts. Furthermore, antioxidants such as catalase, N-acetyl-cysteine or reduced glutathione attenuated COX-2 expression in combined cytokines-treated cells, and also inhibited the activation of ERK, IKK and NF-${\kappa}B$ in MC3T3E1 osteoblasts. In addition, $TNF-{\alpha}$/$IFN-{\gamma}$ stimulated ROS release in the osteoblasts. However, salicylate had no obvious effect on ROS release in DCFDA assay. The results showed that salicylate inhibited the activation of ERK and IKK, $I{\kappa}B$ degradation and NF-${\kappa}B$ activation independent of ROS release and suggested that salicylate exerts its anti-inflammatory action in part through inhibition of ERK, IKK, $I{\kappa}B$, $NF-{\kappa}B$ and resultant COX-2 expression pathway.

Inhibition of Inducible Nitric Oxide Synthase and Cyclooxygenase-2 Activity by $1,2,3,4,6-Penta-Ο-galloyl-{\beta}-D-glucose$ in Murine Macrophage Cells

  • Lee, Sung-Jin;Lee, Ik-Soo;Mar, Woong-Chon
    • Archives of Pharmacal Research
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    • 제26권10호
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    • pp.832-839
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    • 2003
  • Activated macrophages express inducible isoforms of nitric oxide synthase (iNOS) and cyclooxygenase (COX-2), and produce excessive amounts of nitric oxide (NO) and prostaglandin E$_2$ (PGE$_2$), which play key roles in the processes of inflammation and carcinogenesis. The root of Paeonia lactiflora Pall., and the root cortex of Paeonia suffruticosa Andr., are important Chinese crude drugs used in many traditional prescriptions. 1,2,3,4,6-penta-O-galloyl-$\beta$-D-glucose (PGG) is a major bioactive constituent of both crude drugs. PGG has been shown to possess potent anti-oxidant, anti-mutagenic, anti-proliferative and anti-invasive effects. In this study, we examined the inhibitory effects of 1,2,3,4,6-penta-O-galloyl-$\beta$-D-glucose (PGG) isolated from the root of Paeonia lactiflora Pall. on the COX-2 and iNOS activity in LPS-activated Raw 264.7 cells, COX-1 in HEL cells. To investigate the structure-activity relationships of gallate and gallic acid for the inhibition of iNOS and COX-2 activity, we also examined (-)-epigallocatechin gallate (EGCG), gallic acid, and gallacetophenone. The results of the present study indicated that PGG, EGCG, and gallacetophenone treatment except gallic acid significantly inhibited LPS-induced NO production in LPS-activated macrophages. All of the four compounds significantly inhibited COX-2 activity in LPS-activated macrophages. Among the four compounds examined, PGG revealed the most potent in both iNOS ($IC_{50}$ = 18 $\mu\textrm{g}/mL$) and COX-2 inhibitory activity (PGE$_2$: $IC_{50}$ = 8 $\mu\textrm{g}/mL$ and PGD$_2$: $IC_{50}$ = 12 $\mu\textrm{g}/mL$), respectively. Although further studies are needed to elucidate the molecular mechanisms and structure-activity relationship by which PGG exerts its inhibitory actions, our results suggest that PGG might be a candidate for developing anti-inflammatory and cancer chemopreventive agents.

Src Kinase Regulates Nitric Oxide-induced Dedifferentiation and Cyc1ooxygenase-2 Expression in Articular Chondrocytes via p38 Kinase-dependent Pathway

  • Yu, Seon-Mi;Lee, Won-Kil;Yoon, Eun-Kyung;Lee, Ji-Hye;Lee, Sun-Ryung;Kim, Song-Ja
    • IMMUNE NETWORK
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    • 제6권4호
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    • pp.204-210
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    • 2006
  • Background: Nitric oxide (NO) in articular chondrocytes regulates dedifferentiation and inflammatory responses by modulating MAP kinases. In this study, we investigated whether the Src kinase in chondrocytes regulates NO-induced dedifferentiation and cyclooxygenase-2 (COX-2) expression. Methods: Primary chondrocytes were treated with various concentrations of SNP for 24 h. The COX-2 and type II collagen expression levels were determined by immunoblot analysis, and prostaglandin $E_2\;(PGE_2)$ was determined by using a $PGE_2$ assay kit. Expression and distribution of p-Caveolin and COX-2 in rabbit articular chondrocytes and cartilage explants were determined by immunohistochemical staining and immunocytochemical staining, respectively. Results: SNP treatment stimulated Src kinase activation in a dose-dependent manner in articular chondrocytes. The Src kinase inhibitors PP2 [4-amino-5-(4-chlorophenyl)-7-(t-butyl)pyrazolo(3,4-d)pyrimidine], a significantly blocked SNP-induced p38 kinase and caveolin-1 activation in a dose-dependent manner. Therefore, to determine whether Src kinase activation is associated with dedifferentiation and/or COX-2 expression and $PGE_2$ production. As expected, PP2 potentiated SNP-stimulated dedifferentiation, but completely blocked both COX-2 expression and $PGE_2$ production. And also, levels of p-Caveolin and COX-2 protein expression were increased in SNP-treated primary chondrocytes and osteoarthritic and rheumatoid arthritic cartilage, suggesting that p-Caveolin may playa role in the inflammatory responses of arthritic cartilage. Conclusion: Our previously studies indicated that NO caused dedifferentiation and COX-2 expression is regulated by p38 kinase through caveolin-1 (1). Therefore, our results collectively suggest that Src kinase regulates NO-induced dedifferentiation and COX-2 expression in chondrocytes via p38 kinase in association with caveolin-1.

Monitoring of Fasciola Species Contamination in Water Dropwort by COX1 Mitochondrial and ITS-2 rDNA Sequencing Analysis

  • Choi, In-Wook;Kim, Hwang-Yong;Quan, Juan-Hua;Ryu, Jae-Gee;Sun, Rubing;Lee, Young-Ha
    • Parasites, Hosts and Diseases
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    • 제53권5호
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    • pp.641-645
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    • 2015
  • Fascioliasis, a food-borne trematode zoonosis, is a disease primarily in cattle and sheep and occasionally in humans. Water dropwort (Oenanthe javanica), an aquatic perennial herb, is a common second intermediate host of Fasciola, and the fresh stems and leaves are widely used as a seasoning in the Korean diet. However, no information regarding Fasciola species contamination in water dropwort is available. Here, we collected 500 samples of water dropwort in 3 areas in Korea during February and March 2015, and the water dropwort contamination of Fasciola species was monitored by DNA sequencing analysis of the Fasciola hepatica and Fasciola gigantica specific mitochondrial cytochrome c oxidase subunit 1 (cox1) and nuclear ribosomal internal transcribed spacer 2 (ITS-2). Among the 500 samples assessed, the presence of F. hepatica cox1 and 1TS-2 markers were detected in 2 samples, and F. hepatica contamination was confirmed by sequencing analysis. The nucleotide sequences of cox1 PCR products from the 2 F. hepatica-contaminated samples were 96.5% identical to the F. hepatica cox1 sequences in GenBank, whereas F. gigantica cox1 sequences were 46.8% similar with the sequence detected from the cox1 positive samples. However, F. gigantica cox1 and ITS-2 markers were not detected by PCR in the 500 samples of water dropwort. Collectively, in this survey of the water dropwort contamination with Fasciola species, very low prevalence of F. hepatica contamination was detected in the samples.

MP3 압축 공격에 강인한 주파수 계수 분석을 이용한 오디오 워터마킹 (Robust Audio Watermarking Using Frequency Coefficient Analysis for MP3 Compression Attack)

  • 정원교;이경환;우흥체;이용두
    • 한국음향학회지
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    • 제24권8호
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    • pp.492-497
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    • 2005
  • 본 논문에서는 오디오 분야에서 가장 대중적인 압축 방식인 MP3 공격에 강인한 워터마킹 방법을 제안한다. 일반적인 주파수 도메인에서의 워터마킹 방법인 Cox의 스프레드 스펙트럼 방법에서는 DCT후 값이 큰 저주파수의 계수에 순차적으로 워터마크를 삽입한다. 제안한 방법에서는 MP3 공격시 손실되는 주파수 계수를 통계적으로 조사하여, 손실이 덜한 순서를 정한 후 이에 맞추어 계수에 워터마크를 삽입하는 방법을 제안한다. 다양한 음원에 대하여 실험한 결과, 제안한 방법은 Cox의 방법에 비해 워터마크의 보존하고 원본 음원의 왜곡을 줄이는 두가지 측면 모두 좋은 결과를 나타내었다.

잠재적 COX-2 억제작용이 있는 1,5-Diarylhydantoin유도체의 합성 (Synthesis of Potential COX-2 Inhibitory 1,5-Diarylhydantoin Derivatives)

  • 권순경;박해선
    • 약학회지
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    • 제48권2호
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    • pp.135-140
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    • 2004
  • For the development of new COX-2 inhibitors, 1,5-diarylhydantoins 5a∼5c and 1,5-diaryl-2-thiohydantoin 6a∼6c were synthesized from commercially available phenylacetic acids through esterification, bromination, C-N bond formation and cyclization. Esters 2a∼c were efficiently synthesized from the starting materials 1a∼c by refluxing in absolute methanol for 3 hours with catalytic concentrated sulfuric acid. Bromination of 2a∼c was carried out with use of N-bomosuccinimide at rt in dichloromethane. The bromine of 3a∼c was substituted with aniline in ethanol or N,N-dimethylformamide to provide 4a∼c. Hydantoins and 2-thiohydantoins were synthesized from 4a∼c by treatment of potassium isocyanate or potassium thiocyanate in dil-ethanol with triethylamine.

CoMFA and CoMSIA 3D QSAR Studies on Pimarane Cyclooxygenase-2 (COX-2) Inhibitors

  • Lee, Kwang-Ok;Park, Hyun-Ju;Kim, Young-Ho;Seo, Seung-Yong;Lee, Yong-Sil;Moon, Sung-Hyun;Kim, Nam-Joong;Park, Nam-Song;Suh, Young-Ger
    • Archives of Pharmacal Research
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    • 제27권5호
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    • pp.467-470
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    • 2004
  • Comparative molecular field analysis and comparative molecular similarity indices analysis were performed on twenty five analogues of pimarane COX-2 inhibitor to optimize their cyclooxygenase-2 (COX-2) selective anti-inflammatory activities.